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The University of Manchester Research Responsiveness of kinematic and clinical measures of upper-limb motor function after stroke DOI: 10.1016/j.rehab.2020.02.005 Document Version Accepted author manuscript Link to publication record in Manchester Research Explorer Citation for published version (APA): Villepinte, C., Verma, A., Dimeglio, C., Boissezon, X. D., & Gasq, D. (2020). Responsiveness of kinematic and clinical measures of upper-limb motor function after stroke: a systematic review and meta-analysis. Annals of Physical and Rehabilitation Medicine. https://doi.org/10.1016/j.rehab.2020.02.005 Published in: Annals of Physical and Rehabilitation Medicine Citing this paper Please note that where the full-text provided on Manchester Research Explorer is the Author Accepted Manuscript or Proof version this may differ from the final Published version. If citing, it is advised that you check and use the publisher's definitive version. General rights Copyright and moral rights for the publications made accessible in the Research Explorer are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Takedown policy If you believe that this document breaches copyright please refer to the University of Manchester’s Takedown Procedures [http://man.ac.uk/04Y6Bo] or contact [email protected] providing relevant details, so we can investigate your claim. Download date:07. Oct. 2021

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The University of Manchester Research

Responsiveness of kinematic and clinical measures ofupper-limb motor function after strokeDOI:10.1016/j.rehab.2020.02.005

Document VersionAccepted author manuscript

Link to publication record in Manchester Research Explorer

Citation for published version (APA):Villepinte, C., Verma, A., Dimeglio, C., Boissezon, X. D., & Gasq, D. (2020). Responsiveness of kinematic andclinical measures of upper-limb motor function after stroke: a systematic review and meta-analysis. Annals ofPhysical and Rehabilitation Medicine. https://doi.org/10.1016/j.rehab.2020.02.005

Published in:Annals of Physical and Rehabilitation Medicine

Citing this paperPlease note that where the full-text provided on Manchester Research Explorer is the Author Accepted Manuscriptor Proof version this may differ from the final Published version. If citing, it is advised that you check and use thepublisher's definitive version.

General rightsCopyright and moral rights for the publications made accessible in the Research Explorer are retained by theauthors and/or other copyright owners and it is a condition of accessing publications that users recognise andabide by the legal requirements associated with these rights.

Takedown policyIf you believe that this document breaches copyright please refer to the University of Manchester’s TakedownProcedures [http://man.ac.uk/04Y6Bo] or contact [email protected] providingrelevant details, so we can investigate your claim.

Download date:07. Oct. 2021

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Responsiveness of kinematic and clinical measures of upper-limb motorfunction after stroke: a systematic review and meta-analysis

Claire Villepinte OT MSc Arpana Verma MBChB MPH FFPH PhDChloe Dimeglio PhD Xavier De Boissezon MD PhD David Gasq MDPhD

PII: S1877-0657(20)30059-2

DOI: https://doi.org/doi:10.1016/j.rehab.2020.02.005

Reference: REHAB 1366

To appear in: Annals of Physical and Rehabilitation Medicine

Received Date: 29 August 2019

Accepted Date: 15 February 2020

Please cite this article as: Villepinte C, Verma A, Dimeglio C, Boissezon XD, Gasq D,Responsiveness of kinematic and clinical measures of upper-limb motor function after stroke:a systematic review and meta-analysis, Annals of Physical and Rehabilitation Medicine(2020), doi: https://doi.org/10.1016/j.rehab.2020.02.005

This is a PDF file of an article that has undergone enhancements after acceptance, such asthe addition of a cover page and metadata, and formatting for readability, but it is not yet thedefinitive version of record. This version will undergo additional copyediting, typesetting andreview before it is published in its final form, but we are providing this version to give earlyvisibility of the article. Please note that, during the production process, errors may bediscovered which could affect the content, and all legal disclaimers that apply to the journalpertain.

© 2020 Published by Elsevier.

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Responsiveness of kinematic and clinical measures of upper-limb motor function after stroke: a

systematic review and meta-analysis

Abstract

Background. Kinematic analysis and clinical outcome measures with established responsiveness

contribute to the quantified assessment of post-stroke upper-limb function, the selection of

interventions and the differentiation of motor recovery patterns.

Objective. This systematic review and meta-analysis aimed to report trends in use and compare the

responsiveness of kinematic and clinical measures in studies measuring the effectiveness of constraint-

induced movement, trunk restraint and bilateral arm therapies for upper-limb function after stroke.

Methods. In this systematic review, randomised controlled trials implementing kinematic analysis and

clinical outcome measures to evaluate the effects of therapies in post-stroke adults were eligible. We

searched 8 electronic databases (MEDLINE, EMBASE, Web of Science, Scopus, CINAHL, CENTRAL,

OTseeker and Pedro). Risk of bias was assessed according to the Cochrane Risk of Bias domains. A

meta-analysis was conducted for repeated design measures of pre- and post-test data providing

estimated standardised mean differences (SMDs).

Results. We included reports of 12 studies (191 participants) reporting kinematic smoothness,

movement duration and efficiency, trunk and shoulder range of motion, control strategy and velocity

variables in conjunction with assessment by Motor Activity Log, Fugl-Meyer Assessment and Wolf

Motor Function Test. Responsiveness was higher (i.e., non-overlap of 95% confidence intervals [CIs])

for Motor Activity Log score (SMD for amount of use 1.0, 95% CI 0.75–1.25, p<0.001; SMD for quality

of movement 0.96, 95% CI 0.72–1.20, p<0.001) than movement efficiency, trunk and shoulder range

of motion, control strategy and peak velocity.

Conclusion. These results are consistent with current literature supporting the use of combined

kinematic and clinical measures for comprehensive and accurate evaluation of post-stroke

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upper-limb function. Future research should include other design trials and rehabilitation types

to confirm these findings, focusing on subgroup analysis of type of rehabilitation intervention

and functional levels.

Keywords: hemiparesis; upper extremity; kinematics; 3D motion analysis; outcome measure;

psychometrics

Introduction

Upper-limb (UL) impairment due to neurological loss post-stroke typically includes upper

motor neuron syndrome, somatosensory deficit contralateral to the brain lesion and cognitive

disorders [1–3]. Studies estimate that 50% to 85% of individuals with acute stroke and 50%

with chronic stroke present UL impairment [4–6], which influences functional ability in task

accomplishment and independence, thereby affecting quality of life post-stroke [1,7–9].

Studies report a large number of measures used to evaluate UL function. In total, 53 measures

identified contribute to a large diversity in the selection of measures across trials post-stroke

[6,7,10,11]. Clinical guidelines recommend the use of valid, reliable and responsive measures

contributing to evidence-based practice [10,12]. Studies show strong trends in the use of several

measures to evaluate various International Classification of Functioning, Disability and Health

(ICF) levels for UL function post-stroke [6,10,11,13,14]. The use of more than one measure for

several ICF levels is reported in 72% of trials [6]. Discrepancies in the selection of measures

are according to psychometric properties and/or intervention types [6,14]. Knowledge of

psychometric properties of measures will contribute to potential comparisons of treatment

effects [10,15], which will contribute to trial quality and allow for comparison of practices of

studies via meta-analyses contributing to evidence-based care [6,10,13].

The use of psychometrically sound outcome measures contributes to the identification of

appropriate rehabilitation interventions [3,6,7,10,13,16,17]. Generally, the evaluation of

treatment effects in stroke trials depend on the use of observational measures of timed

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standardised tasks [10,18,19]. Measures assessing ICF activity-level function demonstrate

limitations for discriminating motor recovery from motor compensation that is an important

point to consider in constraint-induced movement therapy (CIMT), trunk restraint therapy

(TRT) and bilateral arm therapy (BAT) [8,18,9]. Selection of appropriate interventions should

consider whether outcomes are recovery- or compensatory-based for effects [8–10]. Recovery

is defined as the return of physiological motor patterns with impaired structure, whereas

compensatory movement refers to the ability to accomplish a task through adaptation of motor

patterns [8,9,20].

Discrete strategies of movement and motor impairment may not be detected with clinical

measures [6,21], which indicates a need for more precise measures of compensatory

strategies or subtle impairments [8,19,22,20]. Furthermore, compensatory movement

strategies, such as lateral flexion and forward displacement of the trunk in reaching patterns

are not explicitly measured by most activity-level motor scales, with the exception of the

Wolf Motor Function Test (WMFT) [8,22]. The use of kinematic measures combined with

clinical measures aligned with ICF levels improves the ability to distinguish motor recovery

from compensatory strategies [8,10,13,9].

The use of kinematic measures in UL evaluation is gaining recognition for the measurement of UL

movement in stroke trials, supported by expert-based recommendations [6,13,22,23]. Combined use

of kinematic motion analysis outcomes (KINOs) with clinical outcome measures (CLIOs) contributes to

the differentiation of motor recovery and compensatory movement patterns as well as prognostic

accuracy [6,8,10,22,20,24]. KINOs provide a quantitative and objective measure of UL body function

level according to the ICF [10]. Furthermore, KINOs are well correlated with other clinical measures in

stroke trials, demonstrating high to moderate significant correlation with Fugl-Meyer Assessment for

upper extremity (FMA-UE), Action Research Arm Test (ARAT) and WMFT across reaching tasks

[18,22,25]. The strength of correlations depends on the specific actions that are being measured and

the variable measured in the task [8,22].

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KINOs may present higher responsiveness to change than CLIOs [22,26]. KINOs for assessing

UL post-stroke were present in 21 of 41 trials from 2010 to 2014 [22]. Studies report an

increasing use of KINOs with CLIOs such as the FMA-UE [6] and with activity dexterity

measures providing measurement of impairment of trunk movements in relation to UL tasks

[10,27]. KINO variables have demonstrated established validity and reliability in stroke

populations [10,22,28]; however, responsiveness remains understudied, reported in only 3

trials for movement duration, smoothness, and trunk displacement variables [22,26,28]. In

addition, kinematic analysis has been based on small sample sizes affecting the

generalizability of findings [22,23]. KINO variables may be more precise than clinical

measures, with some studies demonstrating advantages of peak velocity and movement

duration over timed performances of WMFT. However, these variables measured different

aspects of UL movement [10,18]. Other studies demonstrated the ability of KINOs to provide

higher precision of quantitative measurement of specific movement aspects over global

clinical scales assessing broad constructs of UL function [22,25].

Recent recommendations encourage standardisation of kinematic analysis measurement protocols

according to ICF levels, tasks and conditions analysed as well as psychometric properties [10,15,23].

However, evidence regarding KINO responsiveness remains limited [22].

The aim of this systematic review was to establish and compare KINO and CLIO responsiveness for UL

function after post-stroke interventions. Our review sought to first report the effect sizes of KINO and

CLIO changes related to CIMT, TRT, and BAT rehabilitation interventions to conduct the comparison.

Methods

This protocol was registered on the PROSPERO database on March 9, 2016 (registration no.

CRD42015023907).

Literature search

Studies published in English and French were searched in electronic bibliographic databases, subject-

specific databases, and unpublished grey literature, and authors were contacted to identify additional

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studies. Also, reference lists were manually scanned by 2 reviewers independently. The databases

searched were MEDLINE, EMBASE, Web of Science, Scopus, CINAHL, Central Register of Controlled

Trials (CENTRAL), OTSeeker and PEDro. No date limit was imposed in accordance with recent

developments of KINOs [22]. The last search was performed on May 1, 2016, and the literature search

was updated from May 1, 2016 to October 28, 2019.

Specific strategies were used for each database. The MEDLINE strategy is illustrated in Appendix A,

supplementary methods. Index terms used were stroke, upper limb, kinematic and outcome measure.

Methodological filters were used for randomised controlled trial (RCT) designs contributing to a

sensitivity and precision maximising-based search [29].

Selection criteria

Studies were selected according to predetermined eligibility criteria based on Population-

Interventions-Comparator-Outcomes-Study design(s) (PICOS) components [29,30].

Type of participants: Studies of adults ≥ 18 years old with UL impairment post-stroke who underwent

CIMT, TRT and/or BAT interventions were considered. We excluded data for participants who received

other therapies such as functional electric stimulation, robot and/or virtual reality therapy to ensure

the homogeneity of groups for meta-analysis [29]. Neurological conditions other than stroke were

excluded. No exclusion regarding time post-stroke was applied [20].

Types of intervention: Only studies implementing KINOs of UL movement with 3D optoelectronics

motion capture systems were considered because of the high measurement accuracy of free

movements, congruent with recommendations in stroke rehabilitation [22,23,31]. Trials with KINOs

from virtual, robotic or haptic devices were excluded because of the difficulty in comparing data and/or

restriction of UL movements [22,31]. We selected studies reporting KINOs according to established

classifications, including trunk range of motion (ROM), shoulder ROM, elbow ROM, movement

duration, peak velocity, movement efficiency (index of curvature in distal trajectory expressed as a

path ratio), smoothness of movement (number of movement units or peaks on the velocity curve in

distal, the score inversely proportional to smoothness), and control strategy (time of peak velocity

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expressed as a percentage of the movement duration) [22,31]. Studies were excluded if they did not

report at least one of these measurement variables.

Types of comparators: Only studies implementing KINOs in conjunction with CLIOs for UL function post-

stroke were included. CLIOs selected were the most frequently used with high-level psychometric

properties and established clinical utility: FMA-UE, WMFT, ARAT, Chedoke Activity Hand and Arm

Inventory (CAHAI), Motor Activity Log (MAL) and Box and Block Test (BBT) [6,7,10,11]. Studies not

reporting at least one of these measures were excluded.

Types of outcome measures: Responsiveness of KINOs and CLIOs (described above) was computed from

pre- and post-test means and standard deviation values, as a standardised mean difference (SMD)

appropriate for continuous outcomes [29,32].

Study design and setting: Randomised trials reporting at least 2 measurement points (i.e., pre/post)

were included. Studies conducted within clinical, hospital, rehabilitative-based and/or community

settings were included because they contribute to external validity and hence the generalisability of

the results [29].

Study selection and data extraction

Selection of studies was performed independently by 2 reviewers (CV and DG) after screening titles

and abstracts. Studies were included after agreement by reviewers, with discrepancies resolved by a

third author (AV). Duplicate publications were removed after contact with authors and application of

a decision tree [30]. The collection and management of studies was conducted with Zotero

(https://www.zotero.org/) referencing storage and spreadsheet software (Microsoft Office Excel) [33].

The data extraction form was pre-piloted [29] and used independently by 2 reviewers (CV and DG).

Information extracted in accordance with PICOS included characteristics of participants, type of

intervention, modalities of rehabilitation (Table 1), technical aspects of the kinematic evaluation (Table

2), KINOs and CLIOs (Table 3).

Risk of bias

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Risk of bias of studies was determined independently by 2 reviewers (CV and DG) according to the

Cochrane Collaboration Risk of Bias tool [29,30]. Judgement of bias according to the extracted

information was determined as high, low or unclear risk due to lack of information [29]. Data were

extracted by using RevMan 5.3 software. Disagreement between reviewers was resolved by the

arbitrary decision of a third author (AV).

Data analysis

Meta-analyses were performed for continuous summary measures from individual studies with the

SMD calculated by Hedges’ g with 95% confidence intervals (CIs), p values and z scores [29,34]. This

was appropriate for different measurement units for comparison between studies [29,30]. Hedges’ g

was computed for all outcomes as proposed by Borenstein [34] for paired continuous outcomes,

considering the variance of pre- and post-test data. The sign of the post–pre differences was inverted

for outcomes in which improvement is represented as a decrease in score (WMFT Time subscale;

movement smoothness, duration and efficiency; and trunk ROM) to obtain a positive effect size related

to the interventions. Because of lack of availability of correlation (r) data between pre- and post-test

for studies, the pooled effect sizes for r = 0.5 were selected as previously proposed [34]. We performed

a sensitivity analysis using a range of plausible correlations (r = 0, 0.25, 0.5, 0.75 and 0.9) for imputation

of r values for all outcomes, allowing for analysis of the effect of association strength between pre-

and post-test data on the between-studies effect size and between-outcomes responsiveness

[29,34,35].

Meta-analysis of Hedges’ g was performed for each KINO and CLIO across the studies, independent of

the intervention (i.e., CIMT and/or TRT or BAT). Effect sizes were classified as small (<0.2), moderate

(0.2–0.8) or large (>0.8) [30,34]. Heterogeneity or between-study variation of studies was determined

by the I² statistic (low if <50% [29,36]) and visual assessment of forest plots [29]. A random effects

model was systematically applied given the heterogeneous nature of the data collection and the large

variance of the I2 values obtained [37,38]. Forest plots were examined for similarities of the direction

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of treatment effects [39]. Meta-analysis was performed using the package Metafor for R software

[40,41].

Comparison of responsiveness between outcomes involved classification according to the decreasing

value of the pooled Hedges’ g values. With a conservative hypothesis, we considered that a difference

in effect size between 2 outcomes was significant in cases of no overlap of their 95% CIs.

Results

Study selection

A total of 479 articles were identified by the selection procedure presented in Figure 1. After adjusting

for duplicates, 347 studies remained, for which titles and abstracts were screened; 332 studies were

discarded. The full text of 15 studies was assessed for eligibility: 2 studies did not meet the inclusion

criteria in terms of participants [19,25]; one study was a synthesis of 3 RCTs lacking individual results

[43]; and a final study was a duplicate study [25,44]. An additional article was included from the manual

search of reference lists [45]; no relevant unpublished studies were retained [30]. Authors of identified

studies were contacted; however, this did not generate any additional trials. Finally, a total of 12

studies from 2006 to 2015 were identified, some studies including 2 distinct groups in terms of

rehabilitation (CIMT and/or TRT or BAT).

Characteristics of the participants

Characteristics of participants in included studies are shown in Table 1. The mean age of participants

was 56.6 years and the mean time since stroke onset was predominately chronic (>6 months) [20]

across all trials except one [46]: mean 25.7 months (range 11.9 weeks to 21.5 months). Most studies

included participants with mild (57 to 66) to moderate (28 to 57) severity of UL impairment (mean

FMA-UE 46.9/66) [47].

Included studies involved 247 participants who underwent UL rehabilitation, including 128 for CIMT in

8 studies [5,46,48–53], 30 for TRT in 3 studies [45,54,55], 38 for BAT in 2 studies [51,56], and 51 for

CIMT combined with TRT in 4 studies [5,49,52,53].

Intervention characteristics

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Technical aspects of kinematic evaluation are in Table 2. Movement was recorded at spontaneous

velocity across all studies except for one measuring maximal velocity [53], and 2 studies recorded both

(data were analysed at spontaneous velocity) [51,56]. UL evaluation was assessed across unimanual

functional tasks including reaching, point-to-point or reach-to-grasp with objects (a bell or can)

[5,45,46,48–56], and 3 trials analysed bimanual tasks in both reaching and activities of daily living

(opening a box or drawer and retrieving a note; not retained for data analysis) [50,51,56]. The

evaluations retained for data analysis were systematically performed at the end of the rehabilitation

programme.

Kinematic outcomes

KINOs are shown in Table 3. Trunk ROM was assessed in 7 trials but reported in 6 describing TRT with

or without additional CIMT [5,45,49,52–54] (data not usable from the study by Michaelsen et al.,

2006). Values were calculated from sagittal trunk displacement and often standardised by hand

movement indicating the ratio of trunk to UL movement. Data from one study was not included [53]

because of calculation according to 3 phases of the reaching movement. Five studies measured

shoulder ROM: 2 after TRT [54,57] and 3 CIMT+TRT studies [49,52,53] with a predominance of shoulder

flexion. Seven studies assessed elbow ROM after TRT, CIMT and CIMT+TRT, including one for which

the data were not usable [55]. Four reports described metrics from 2 subgroups of TRT [45,54], 1

subgroup of CIMT [46], and 1 subgroup of CIMT/BAT [51]. Movement efficiency, movement duration

and control strategy were the most reported, in 7 trials [5,46,49,54–56]. Smoothness was measured

in 6 studies [46,48,49,51,54,55] among all intervention subgroups.

Clinical outcomes

CLIOs are shown in Table 3. Three studies reported the use of only one CLIO [48,50,54], either FMA-

UE or MAL. Use of more than one ICF level measure was reported in the remaining studies. FMA-UE

impairment measure, for all intervention subgroups, was used in 7 studies, but the data were reported

in only 6 trials, for which 5 reported the combined use with an activity level measure including MAL,

WMFT and/or BBT. All 9 studies reporting CIMT included MAL activity measures [5,46,48–52,56], used

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with other impairment and activity level measures in 7 studies. The activity measure WMFT was used

in 3 studies [5,49,51] across all interventions. ARAT and BBT were the least reported measures for

CIMT+TRT and TRT, respectively. No studies reported the use of CAHAI.

Risk of bias within studies

Risk of bias for included studies is in Figure 2. A detailed description of risk of bias for individual studies

is in Appendix A, supplementary results – risk of bias in studies.

Results of individual studies

Raw values and results of meta-analyses for KINO and CLIO summary measures from individual studies

(SMD calculated by Hedges’ g with 95% CIs, p values, z-scores, heterogeneity and forest plots) are in

Appendix A, supplementary results – individual studies meta-analyses.

Primary outcomes: kinematic measures

All KINOs demonstrated statistically significant responsiveness, except for trunk ROM. We found

statistically significant moderate pooled effect estimates demonstrating improvement in post-test

scores overall for smoothness (Fig. A1), movement duration (Fig. A2; improvement expressed as

reduction in time scores), peak velocity (Fig. A3), shoulder ROM (Fig. A4), control strategy (Fig. A5) and

movement efficiency (Fig. A6; expressed as a reduction in the measure, hence a negative value). Elbow

ROM (Fig. A7) demonstrated a statistically significant small to moderate improvement in pooled effect

estimate post-test scores, but trunk ROM (Fig. A8) did not demonstrate a statistically significant

improvement in pooled effect estimate post-test scores.

Clinical outcomes measures

All CLIOs demonstrated statistically significant responsiveness. The MAL questionnaire subscales

amount of use (AOU) (Fig. A9) and quality of movement (QOM) (Fig. A10) demonstrated large

statistically significant effect sizes for post-test measures. FMA-UE (Fig. A11), WMFT Time subscale

(Fig. A12; expressed as a reduction to indicate improvement) and WMFT Quality (Fig. A13) score

variables demonstrated statistically significant moderate improvement of the pooled effect estimate.

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ARAT and BBT were reported in only one trial, so meta-analysis was inappropriate. BBT reported in a

TRT subgroup [57] (n=15) demonstrated significant improvement (p<0.01), but no CI was provided.

Improvements of the activity measure ARAT was reported [53] in CIMT+TRT (n=20) and CIMT (n=19)

groups (p<0.05), but no CI was provided. No studies reported the use of the CAHAI to measure UL

functional capacity in conjunction with KINO analysis post-stroke.

Comparison of responsiveness of KINOs and CLIOs

Comparison of the pooled effect estimates of SMDs calculated by Hedges’ g (95% CI) for individual

KINOs and CLIOs are shown in Figure 3. Comparison of pooled effect estimates enabled identification

of the strength of change after interventions.

No statistical difference of responsiveness can be assumed between measures, except for MAL AOU

and QOM over KINO movement efficiency, trunk ROM, shoulder ROM, control strategy and peak

velocity due to absence of overlapping CIs.

Smoothness was the most responsive KINO, with the highest moderate estimated effect size, whereas

the FMA-UE clinical measure of UL structure and function demonstrated similar responsiveness. In

descending order of responsiveness effect sizes, moderate effect sizes were demonstrated across

WMFT Time measure, movement duration, WMFT Quality, peak velocity, and shoulder ROM, followed

by movement efficiency, control strategy and elbow ROM. Finally, trunk ROM did not demonstrate

significant responsiveness.

Sensitivity analysis

The sensitivity analysis conducted with different correlation values of pre–post measures for

calculation of the between-outcomes summative effect size (i.e., responsiveness for KINOs and CLIOs)

revealed that the analyses with r = 0.5 were robust. Changing the correlations had a negligible impact

on the results (Table A1 in Appendix A, supplementary results – sensitivity analysis).

Discussion

The main finding of this review was the reporting and comparison of responsiveness of UL stroke

outcome measures as determined by treatment effect sizes of pre-test/post-test measurements, after

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CIMT, TR, CIMT+TR and BAT rehabilitation. Thirteen KINO (n=8) and CLIO (n=5) outcome measures

were identified, which allowed for a comparative overview of meta-analysis results. All measures

demonstrated significant statistical improvements, with the exception of trunk ROM. Responsiveness

of kinematic variables was identified for use in clinical trials and practice, filling a gap identified in the

literature [22]. Information regarding psychometric properties of KINO measures will assist in the

selection of clinically relevant kinematic variables appropriate for intervention studies and practice

[22].

Comparison of responsiveness between outcomes measures

MAL activity measure was present among all 9 studies reporting CIMT [5,46,48–52,56]. The

responsiveness of MAL AOU and QOM was greater than peak velocity, shoulder ROM, movement

efficiency, control strategy, elbow ROM and trunk ROM. Comparison of effect sizes of kinematic and

clinical outcomes measures demonstrated homogenous responsiveness as demonstrated by overlap

of 95% CIs [42]. Contrary to previous studies of similar populations, responsiveness of KINOs was not

greater than CLIOs after CIMT, TR, CIMT+TR and BAT in patients with chronic stroke [13,22,26] and no

advantage of peak velocity and movement duration was demonstrated over WMFT Time [10,18]. This

discrepancy can be explained by the greater statistical power of the meta-analysis as compared with

individual studies.

Consideration of subjective measures

The subjective dimension of the MAL questionnaire should be highlighted in terms of the influence of

treatment effects leading to effect sizes larger than the more objective measures, based on actual

performance [7,58,59]. This finding illustrates potential overestimation by subjective measures on

treatment effects contributing to the risk of bias in outcome assessment [6,11,29]. The benefit of

interventions judged by a subjective questionnaire (i.e., MAL scores) appeared greater than that

judged by objective outcomes measures (i.e., kinematic data or scales with standardized rating by a

therapist). This finding raises questions for future research to compare MAL to quantitative ecological

observational measures [1,6], highlighting the importance of using MAL combined with outcome

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measures of various ICF levels to ensure objective and comprehensive evaluation of UL impairment on

activities of daily living [6,7,10,11].

Trends and combination of measure selection

CLIOs: FMA-UE was the most reported measure combined with kinematic analysis, which is consistent

with findings supporting its use for assessing body function and structure in conjunction with activity

ICF measures, as a predominant consensus post-stroke [6,10,13]. Trends of ICF activity-measure use

across trials varied. Despite emerging international consensus supporting the use of ARAT [13], it was

reported in only one study [52]. Trends of WMFT and BBT use, reported in 2 and 1 studies, respectively,

are consistent with reviews identifying the highest frequency of use among these measures with ARAT

and MAL [6,10]. Despite well-established psychometric properties in post-stroke rehabilitation [10],

CAHAI was not reported in conjunction with KINOs.

KINOs: Movement duration, efficiency and control strategy were the most reported kinematic

variables, followed by smoothness, elbow ROM, peak velocity, shoulder ROM and trunk displacement.

KINO selection was consistent with findings among stroke populations across 93 intervention,

comparative and longitudinal trials [22]. Our findings are consistent with recommendations for the use

of measures in conjunction with ICF levels [6,7,10].

Although the literature recommends measure classification according to ICF levels, time since stroke,

measurement type and psychometric properties, the responsiveness of KINO variables remains

understudied [6,13,22]. Increased use of kinematic analysis in UL evaluation highlights a need to

standardise analysis methods and the identification of best-fit variables for specific interventions and

prediction of recovery, encouraging their potential use across clinical practice [10,15,19,22].

Limitations

The lack of availability of data from studies, despite contact with authors, did not provide sufficient

information for potential imputation of correlation values appropriate to repeated-measures analysis

methodology. Restriction of study selection to English and French publications may have contributed

to a language bias [29,30]. Despite application of a duplicate publication decision tree [30], multiple

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publication bias may have influenced results. Even if predefined inclusion criteria and RCT design

selection contributed to comparability and synthesis of results [29], evidence can only be generalised

to CIMT, TRT and BAT interventions using 3D optoelectronic movement analysis systems [22]. Variation

of data acquisition conditions across studies, such as number of trials, task analysed (e.g., reaching

with or without grasping) and/or sampling rate, may have affected the comparability of effect sizes

[9,22,23]. Studies had low or unclear bias, with the exception of 2 studies presenting high risk of bias

in conjunction with small sample sizes. The conclusions of this work cannot be extrapolated to

kinematic data obtained from virtual, robotic or haptic devices, which were not retained in our analysis

in order to limit the heterogeneity of the data.

Conclusions

This study has highlighted current trends of measure selection for evaluating UL function post-stroke

after CIMT, BAT and TRT. Findings support the combined use of kinematic analysis and clinical outcome

measures aligned with ICF levels for assessment. We identified the use of the FMA-UE measure for

assessing ICF body function level, which supports international consensus. Variations in the use of ICF

activity level measures indicate that further consensus is needed regarding their use across trials.

Furthermore, the effect of objective (i.e., kinematic data or scales with standardized rating by a

therapist) or subjective (i.e., self-reported questionnaire) nature of outcomes measures on treatment

effects should be considered in trials, because findings confirm that subjective measures

demonstrated greater perceived benefits. Kinematic variables did not have higher levels of

responsiveness over objective clinical outcome measures in adults with chronic stroke. However,

unlike the CLIOs, they have the advantage of characterizing the quality and structure of the movement,

leading to a better understanding of the underlying neural mechanisms of functional improvements

[9].

Further research should include various study designs, rehabilitation techniques and times post-stroke

to enable further investigation for use of standardised kinematic variables. The development of

wearable, inexpensive and easy-to-use kinematic analysis devices could promote their dissemination

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[23]. Consensus will contribute to the identification of clinically significant changes contributing to

evidence-based practice. Future research of kinematic-variable responsiveness for stroke

rehabilitation should highlight the potential use of combined evaluative methods, demonstrating

psychometric qualities for composite scores of UL function combined with ICF components.

Acknowledgements. The authors acknowledge the authors of the included studies in the review who

provided us with additional information enabling data analysis.

Conflict of interest. None declared.

Funding. This research did not receive any specific grant from funding agencies in the public,

commercial, or not-for-profit sectors.

Figure legends

Figure 1: PRISMA flow diagram of study selection.

Figure 2: Risk of bias of studies assessed with the Cochrane Collaboration Risk of Bias tool.

Figure 3: Responsiveness assessed by comparing meta-analysis pooled effect estimates of

standardised mean difference obtained with a correlation coefficient of 0.5 between pre- and post-

test paired data for individual KINOs and CLIOs (CI, confidence interval; CLIO, clinical outcome

measures; FMA-UE, Fugl-Meyer Assessment - Upper Extremity; KINO, kinematic outcome measures;

MAL, Motor Activity Log; AOU, amount of use; QOM, quality of movement; ROM, range of motion;

WMFT, Wolf Motor Function Test).

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